Canonical Allele Identifier: CA2585296553

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342392-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342392_41342393insAA , CM000681.2:g.41342392_41342393insAA	GRCh38
NC_000019.9:g.41848297_41848298insAA , CM000681.1:g.41848297_41848298insAA	GRCh37
NC_000019.8:g.46540137_46540138insAA	NCBI36
NG_013364.1:g.16534_16535insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-146_635-145insTT MANE Select	ENSP00000221930.4:n.635-146_635-145insTT
ENST00000600196.2:c.635-146_635-145insTT	ENSP00000504008.1:n.635-146_635-145insTT
ENST00000677934.1:c.634+2354_634+2355insTT	ENSP00000504769.1:n.634+2354_634+2355insTT
ENST00000221930.5:c.635-146_635-145insTT	ENSP00000221930.4:n.635-146_635-145insTT
ENST00000597453.1:n.166-146_166-145insTT
ENST00000600196.1:n.95-146_95-145insTT
NM_000660.5:c.635-146_635-145insTT	NP_000651.3:n.635-146_635-145insTT
XM_011527242.1:c.635-146_635-145insTT	XP_011525544.1:n.635-146_635-145insTT
NM_000660.6:c.635-146_635-145insTT	NP_000651.3:n.635-146_635-145insTT
XM_011527242.2:c.635-146_635-145insTT	XP_011525544.1:n.635-146_635-145insTT
NM_000660.7:c.635-146_635-145insTT MANE Select	NP_000651.3:n.635-146_635-145insTT